Allele Registry

Canonical Allele Identifier: PA125254

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016653

RCV000759802

ClinVar Variation:

15399

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Asp22Tyr	CA125253 NM_000518.5:c.64G>T